Nuclear Medicine Research Outsourcing Services

Our nuclear medicine research outsourcing services support the design, synthesis, quality control, and clinical validation of diagnostic and therapeutic radioisotopes, advancing precise molecular imaging and radionuclide therapy.

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Our Nuclear Medicine Research Capabilities

Our radiochemists and nuclear imaging specialists use advanced cyclotron production, radiolabeling technologies, and in vivo imaging models to develop and test safe, effective nuclear medicine agents.

Types of Nuclear Medicine Research We Handle

Radiopharmaceutical Synthesis
Radioisotope Labeling and Optimization
SPECT Tracer Development
PET Radiotracer Synthesis
Theranostic Agent Development
Radiochemical Purity Assessment
Radiation Dosimetry Modelling
Pharmacokinetic Studies of Radioagents
In Vivo Biodistribution Studies
Targeted Radionuclide Therapy Research
Radiolabeled Antibody Development
Peptide-Based Radiotracer Studies
Beta and Alpha Emitting Isotope Validation
Nanoparticle Radio-Labeling
Quality Assurance of Imaging Agents
Preclinical SPECT/PET Imaging
Autoradiography for Tissue Distribution
Dosimetry and Safety Profiling
Radionuclide Generator Evaluation
Isotope Stability Testing
Good Radiopharmacy Practice (GRPP)
Clinical Trial Radiopharmaceutical Support
Regulatory Documentation for Radio Drugs
Cross-Species Pharmacodynamics Studies
Publication-Ready Nuclear Medicine Data
Regulatory-Compliant Nuclear Reports
Cross-Lab Collaborative Nuclear Projects
Customized Nuclear Medicine Research
Radioactive Waste Handling and Safety
Scale-Up Feasibility for Radiopharmaceuticals

Key Research Outsourcing Services Offered

Radioisotope Sourcing and Cyclotron Support
Radiolabeling Method Development
Radiochemical Purity Testing (HPLC, TLC)
Pharmacokinetic and Biodistribution Assays
Dosimetry Calculations and Modelling
In Vivo SPECT/PET Imaging Studies
Theranostic Agent Validation
Radiolabeled Antibody Conjugation
Peptide and Nanoparticle Labeling
Preclinical Animal Model Studies
Autoradiography and Histopathology
Radiation Safety Compliance Audits
Good Radiopharmacy Practice Support
Batch Production and QC Documentation
Regulatory Filing Assistance
Confidential Data Handling and NDA
Interim Progress Reports
Publication-Ready Figures and Datasets
Stakeholder Presentation Support
Workshops and Training in Nuclear Medicine
Post-Project Technical Consulting
IP and Patent Filing Support
Grant Proposal and Manuscript Assistance
Sample Archiving and Secure Backup
Compliance with GLP, GCP, ISO Standards
Cross-Lab Data Validation and Sharing
Collaboration with Nuclear Medicine Centers
Long-Term Nuclear Medicine Partnerships
Scale-Up and Commercialization Feasibility

Why Choose Us for Nuclear Medicine Research Outsourcing?

Our experts deliver robust radiopharmaceutical data, validated dosimetry profiles, and regulatory-ready reports, enabling your diagnostics or therapy agents to reach market faster and safer.

Industries & Sectors We Serve

Clinical Nuclear Medicine Departments
Radiopharmaceutical Companies
Academic Radiology and Imaging Institutes
Oncology Research Centers
Regulatory Radiopharmacy Units
Theranostic R&D Divisions

Customized Nuclear Medicine Solutions

We design radiolabeling protocols, dosimetry plans, and safety assessments tailored to your diagnostic or therapeutic radioagent development needs.

Quality Assurance & Regulatory Compliance

Our workflows comply with GLP, GCP, ISO, and IAEA safety standards, ensuring reproducible, validated, and audit-ready nuclear medicine research outputs.

Case Studies & Client Success Stories

Discover how our outsourcing has advanced new PET tracers, improved dosimetry for therapeutic isotopes, and accelerated regulatory approval for radiopharmaceuticals. References available on request.

How It Works: Our Research Outsourcing Process

Requirement Gathering: Define radioisotope, therapeutic target, and study endpoints.
Proposal & Quotation: Provide detailed plan, compliance roadmap, timeline, and budget.
Lab Execution: Perform synthesis, radiolabeling, QC, and preclinical validation.
Reporting: Deliver data packages, regulatory documents, and compliance-ready reports.
Post-Project Support: Offer scale-up consulting, IP protection, and publication help.

Frequently Asked Questions (FAQs)

Q: Do you synthesize custom PET and SPECT tracers?
A: Yes — we develop and validate novel tracers for diagnostics and therapy applications.

Q: Can you handle dosimetry modeling?
A: Absolutely — we provide robust dosimetry calculations and safety profiling for regulatory submissions.

Q: How secure is my radiopharmaceutical data?
A: Strict NDAs, secure storage, and full compliance with radiological safety standards protect your data.

Get Started / Request a Quote

Contact us today to discuss your nuclear medicine project and receive a custom plan, timeline, and cost estimate aligned with your clinical and regulatory goals.